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Recruiting Not applicable NCT03217006

Randomization of Single vs Multiple Arterial Grafts

No applicable phase (e.g. observational)
Conditions: Coronary Artery Disease Heart Diseases

Sponsor: Weill Medical College of Cornell University

trial.available_in: БГ
Overview
The primary hypothesis of ROMA is that in patients undergoing primary isolated non-emergent coronary artery bypass surgery (CABG), the use of two or more arterial grafts compared to a single arterial graft is associated with a reduction in the composite outcome of death from any cause, any stroke, post discharge myocardial infarction and/or repeat revascularization. The secondary hypothesis is that in patients undergoing primary isolated non-emergent CABG, the use of two or more arterial grafts compared to a single arterial graft is associated with improved survival. Prospective event-driven unblinded randomized multicenter trial of at least 4,300 subjects enrolled in at least 25 international centers. Patients will be randomized to a single arterial graft (SAG) or multiple arterial grafts (MAG). Patients will be randomized in a 1:1 fashion between the two groups. Permuted block randomization with random blocks stratified by the center and the type of second arterial graft will be used to provide treatment distribution in equal proportion.
Description
In the 1980's, it was recognized that long-term survival was enhanced in patients undergoing coronary surgery when the left anterior descending (LAD) was grafted with a left internal thoracic artery (ITA) rather than a saphenous vein (1). This difference was predicated, at least in part, due to greater and more durable patency of the left ITA compared to an increased early occlusion rate and later progressive atherosclerosis of saphenous vein grafts (SVG) (2). For more than 20 years it has generally been accepted that patients who receive multiple arterial grafts (AGs) at the time of coronary artery bypass surgery (CABG) have increased postoperative survival compared to those who receive only one AG, especially over the long term (3-5). The current United States and European Guidelines encourage the use of AGs in patients with a long life expectancy (6, 7). Last year, a position paper from the Society of Thoracic Surgeons strongly recommended a wider use of AGs (8). The putative mechanism underlying the AG hypothesis is greater patency. In line with the original findings of improved LAD graft patency with ITA vs. SVG, data from randomized control trials (RCTs) as well as observational studies and a network meta-analysis (9) have demonstrated that the patency of the RA, as well as the right ITA, exceed that of a SVG, providing mechanistic basis to support the AG hypothesis. ROMA is a two arm event driven randomized multi-centre trial aimed at evaluating the impact of the use of one ITA vs two or more AGs for CABG on a composite of death from any cause, any stroke, post discharge myocardial infarction and/or repeat revascularization. The trial is powered to detect a 20% relative reduction in the primary outcome with 90% power at 5% alpha. The primary aim is to conduct a multicenter international randomized control trial to test the hypothesis that the use of a two or more AGs compared to a single arterial graft is associated with a reduction in the composite outcome of death from any cause, any stroke, post discharge myocardial infarction and/or repeat revascularization. The secondary aim is to conduct a multicenter international randomized control trial to test the hypothesis that the use of two or more AGs compared to a single arterial graft is associated with improved survival.
Who can participate
Inclusion Criteria: * Primary isolated CABG patients with disease of the left main coronary artery and/or of the left anterior descending and the circumflex coronary system with or without disease of the right coronary artery. Exclusion Criteria: * Age \> 70 years * Single graft * Emergency operation * Evolving myocardial infarction within 48 hours of surgery * Left ventricular ejection fraction of \< 35% * Any concomitant cardiac or non-cardiac procedure * Previous cardiac surgery * Preoperative severe end-organ dysfunction (dialysis, liver failure, respiratory failure), cancer or any co-morbidity that reduce life expectancy to less than 5 years. * Inability to use the saphenous vein or to use both radial and right internal thoracic arteries * Anticipated need for coronary thrombo-endarterectomy * Planned hybrid revascularization
Interventions
Single arterial graft
PROCEDURE
Multiple arterial grafting
PROCEDURE
Locations 59
Austria (3)
Innsbruck (Medical University) Austria
Innsbruck
Elfriede Ruttmann-Ulmer
Krankenhaus Nord Vienna North Hospital
Vienna
MU Vienna Austria
Vienna
Brazil (1)
Federal University of Sao Paulo
São Paulo
Canada (9)
Hamilton General Hospital
Hamilton
London Health Sciences Ontario Canada
London
University Hospital of Montreal (CHUM)
Montreal
University of Ottawa Heart Institute Canada
Ottawa
Royal Victoria Hospital (McGill)
Québec
Universite Laval Quebec (CRIUCPQ) Canada
Québec
Sunnybrook Health Sciences Centre
Toronto
Toronto General Hospital
Toronto
St. Boniface General Hospital / WHRA
Winnipeg
China (5)
Fuwai Hospital
Beijing
Jilin Heart Hospital
Changchun
Ruijin Hospital Shanghai Jiao Tong University School of Medicine
Shanghai
National Taiwan University Hospital
Taiwan
Yih-Sharng Chen
Teda Hospital (TICH)
Tianjin
Guo-Wei He
Croatia (1)
University Hospital Dubrava
Zagreb
Igor Rudez
Czech Republic (1)
General University Hospital, Prague
Prague
Germany (11)
Duisburg Heart Center
Duisburg
Essen University
Duisburg
Matthias Klaus Thielmann
Düsseldorf University
Düsseldorf
University Hospital Erlangen
Erlangen
Giessen Hospital
Giessen
University Medical Center of Goettingen
Göttingen
ENROLLING_BY_INVITATION
Jena University Hospital
Jena
Heart Center (Herzzentrum)
Leipzig
HDZ NRW Bad
Oeynhausen
Kavous Haikim- Meibodi
Robert-Bosch-Hospital
Stuttgart
Krankenhaus der Barmherzigen Brüder Trier
Trier
Italy (6)
Anthea Hospital
Bari
Giuseppe Speziale
Fondazione Poliambulanza
Brescia
Maria Cecilia Hospital GVM
Cotignola
Universita' Cattolica del Sacro Cuore
Roma
European Hospital
Rome
Ruggero De Paulis
Ospedale Le Molinette
Torino
Japan (1)
Saitama Medical University
Saitama
Hiroyuki Nakajima
Netherlands (1)
MUMC Maastricht (University Medical Centre)
Maastricht
Poland (1)
Medical University of Silesia (Katowice)
Katowice
Portugal (3)
Hospitalar de Lisboa Central
Capuchos
University Hospital (Praceta Mota Pinto)
Coimbra
Manuel Antunes
Centro Hospitalar e Universitário São João
Porto
Serbia (1)
Dedinje Cardiovascular Institute
Belgrade
Singapore (1)
National University of Singapore
Singapore
South Korea (1)
Severance Cardiovascular Hospital, Yonsei University College of Medicine
Sinchŏn-dong
Kyung-Jong Yoo
Spain (2)
Hospital Univeritario Del Vinalopo
Alicante
Hospital Clinic de Barcelona (ICCV)
Barcelona
United States (11)
University of Colorado
Boulder , Colorado
NewYork-Presbyterian Brooklyn Methodist Hospital
Brooklyn , New York
Cleveland Clinic Foundation
Cleveland , Ohio
Faisal Bakaeen
Nebraska Heart Hospital
Lincoln , Nebraska
Icahn School of Medicine, Mount Sinai
New York , New York
Weil Cornell Medical College Department of Cardiothoracic Surgery
New York , New York
Lenox Hill Hospital (Northwell)
New York , New York
NewYork-Presbyterian Queens
New York , New York
University of Nebraska Medical Center
Omaha , Nebraska
Allegheny General Hospital (Cardiovascular Institute)
Pittsburgh , Pennsylvania
Baystate Health
Springfield , Massachusetts
Technical details
Status
Recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Maximum age
70 Years
Healthy volunteers
No
Start date
07.01.2018
Completion date
01.01.2030
Registry ID
NCT03217006
Source
clinicaltrials.gov
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